- Coumermycin A1
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Coumermycin A1 Systematic (IUPAC) name [(3R,4S,5R)-5-Hydroxy-6-[2-hydroxy-3-[[4-[[2-hydroxy-7-[(3R,4S,5R)-3-hydroxy-5-methoxy-6,6-dimethyl-4-(5-methyl-1H-pyrrole-2-carbonyl)oxyoxan-2-yl]oxy-8-methyl-4-oxochromen-3-yl]carbamoyl]-3-methyl-1H-pyrrole-2-carbonyl]amino]-8-methyl-4-oxochromen-7-yl]oxy-3-methoxy-2,2-dimethyloxan-4-yl] 5-methyl-1H-pyrrole-2-carboxylate Clinical data Pregnancy cat. ? Legal status ? Identifiers CAS number 4434-05-3 ATC code None PubChem CID 451651 ChEMBL CHEMBL555830 Synonyms Coumamycin Chemical data Formula C55H59N5O20 Mol. mass 1110.08 g/mol SMILES eMolecules & PubChem (what is this?) A1 (verify) Coumermycin A1 is an aminocoumarin.[1][2]
References
- ^ Heide, L. (2009). "Genetic engineering of antibiotic biosynthesis for the generation of new aminocoumarins". Biotechnology advances 27 (6): 1006–1014. doi:10.1016/j.biotechadv.2009.05.017. PMID 19463934.
- ^ Heide, L.; Gust, B.; Anderle, C.; Li, S. M. (2008). "Combinatorial biosynthesis, metabolic engineering and mutasynthesis for the generation of new aminocoumarin antibiotics". Current Topics in Medicinal Chemistry 8 (8): 667–679. doi:10.2174/156802608784221505. PMID 18473891.
Other/ungroupedCombinationsTopoisomerase
inhibitors/
quinolones/
(inhibits
DNA replication)1st g.2nd g.Ciprofloxacin# • Enoxacin‡ • Fleroxacin‡ • Lomefloxacin • Nadifloxacin • Ofloxacin • Norfloxacin • Pefloxacin • Rufloxacin3rd g.4th g.Besifloxacin • Clinafloxacin† • Garenoxacin • Gemifloxacin • Moxifloxacin • Gatifloxacin‡ • Sitafloxacin • Trovafloxacin‡/Alatrofloxacin‡ • PrulifloxacinVet.Related (DG)Anaerobic DNA
inhibitorsNitrofuran derivativesRNA synthesis Categories:- Antibiotic stubs
- Antibiotics
- Imidazoles
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